A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534426



Internal ID20907787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21275696..21281826hg38UCSC Ensembl
chr20:21256334..21262464hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg386131
hg196131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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